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Early CPAP Intervention Improves Cognition and Function in Stroke Patients with OSA: Predictive Roles of Serum NfL and GFAP as Biomarkers

Early CPAP Intervention Improves Cognition and Function in Stroke Patients with OSA: Predictive Roles of Serum NfL and GFAP as Biomarkers

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110921
Enrollment
Unknown
Registered
2025-10-22
Start date
2025-10-30
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

This study focused on the comorbidity population of acute ischemic or hemorrhagic stroke and obstructive sleep apnea (OSA). The core of the study focuses on two core syndromes that are caused or exacerbated by this comorbid state: post-stroke cognitive impairment (PSCI), which manifests as difficulty concentrating, memory loss, impaired executive function, and slowed information processing

Interventions

Control group:Conventional treatment
Treatment group:Continuous positive airway pressure

Sponsors

Northwestern University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Acute cerebral infarction diagnosed by CT or MRI; 2. Meet the diagnostic criteria of the International Classification of Sleep Disorders-third edition (ICSD-3) and meet the diagnostic criteria for OSA in adults: the following 1) 2) 3) are required. (1) At least one of the following manifestations: 1) complaints of drowsiness, non-restorative sleep, fatigue or insomnia; 2) waking up from sleep due to holding breath or wheezing; 3) Residents in the same dormitory or other witnesses report habitual snoring, interruption of breathing, or both during sleep; 4) Confirmed hypertension, mood disorders, cognitive impairment, coronary heart disease, cerebrovascular disease, congestive heart failure, atrial fibrillation, or type 2 diabetes. (2) PSG or out-of-center sleep test (OCST) confirmed that respiratory events occurred during >= 5 times/hour during the monitoring period, including obstructive apnea, mixed apnea, hypopnea, and respiratory effort-related awakenings. (3) PSG or OCST confirmed that respiratory events occurred during >= 15 times/hour during monitoring, including obstructive apnea, mixed apnea, hypopnea, and RERAs, and patients with an AHI >= 20/h. 3. Age 18-80 years old; 4. within 2 weeks after the onset of stroke; 5. Clear consciousness and able to complete simple instructions; 6. Patients who provide informed consent.

Exclusion criteria

Exclusion criteria: 1. History of traumatic brain injury or brain tumor; 2. Diagnosis of mild obstructive sleep apnea (OSA) or central sleep apnea or mixed sleep apnea; 3. Baseline oxygen saturation < 95%; 4. Acute or chronic cardiopulmonary disease affecting lung function; 5. Presence of neuromuscular diseases (such as amyotrophic lateral sclerosis and muscle weakness); 6. Patients with severe dysfunction of other important organs and unstable condition.

Design outcomes

Primary

MeasureTime frame
PSG detection;NfL and GFAP levels;Cognitive and functional assessments;

Secondary

MeasureTime frame
Basic information collection;

Countries

China

Contacts

Public ContactZhao Rongjian

Northwestern University First Hospital

z42423823@163.com+86 29 8365 7930

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026